Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10480 | A01 | 4801946 | C | T | downstream_gene_variant | MODIFIER | c.*4164G>A| |
S230 |
2 | BAA01g10480 | A01 | 4802059 | T | C | downstream_gene_variant | MODIFIER | c.*4051A>G| |
S207 S248 S49 S71 |
3 | BAA01g10480 | A01 | 4803040 | C | T | downstream_gene_variant | MODIFIER | c.*3070G>A| |
S211 S227 |
4 | BAA01g10480 | A01 | 4803884 | G | A | downstream_gene_variant | MODIFIER | c.*2226C>T| |
S308 |
5 | BAA01g10480 | A01 | 4803918 | C | T | downstream_gene_variant | MODIFIER | c.*2192G>A| |
S38 |
6 | BAA01g10480 | A01 | 4804812 | G | A | downstream_gene_variant | MODIFIER | c.*1298C>T| |
S146 S212 S259 S69 |
7 | BAA01g10480 | A01 | 4804910 | G | A | downstream_gene_variant | MODIFIER | c.*1200C>T| |
S56 |
8 | BAA01g10480 | A01 | 4806289 | G | A | splice_region_variant&intron_variant | LOW | c.1336-3C>T| |
S199 |
9 | BAA01g10480 | A01 | 4806381 | G | A | missense_variant | MODERATE | c.1316C>T|p.Thr439Ile |
S280 |
10 | BAA01g10480 | A01 | 4806467 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1231-1G>A| |
S158 |
11 | BAA01g10480 | A01 | 4807051 | G | A | synonymous_variant | LOW | c.942C>T|p.Gly314Gly |
S201 |
12 | BAA01g10480 | A01 | 4808171 | G | A | missense_variant | MODERATE | c.155C>T|p.Thr52Ile |
S139 |
13 | BAA01g10480 | A01 | 4808951 | G | A | upstream_gene_variant | MODIFIER | c.-202C>T| |
S180 |
14 | BAA01g10480 | A01 | 4809615 | G | A | upstream_gene_variant | MODIFIER | c.-866C>T| |
S8 |
15 | BAA01g10480 | A01 | 4810540 | G | A | upstream_gene_variant | MODIFIER | c.-1791C>T| |
S72 S78 |
16 | BAA01g10480 | A01 | 4812333 | A | T | upstream_gene_variant | MODIFIER | c.-3584T>A| |
S302 |